MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE— 510(k) K915441
Substantially EquivalentFisher Scientific Co., LLC
FDA 510(k) clearance K915441 for MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE, Substantially Equivalent on 1992-01-08. Applicant: Fisher Scientific Co., LLC. Device class: 2.
Clearance details
- Applicant
- Fisher Scientific Co., LLC
- Product code
- Code GKF
- Device class
- Class 2
- Regulation
- 21 CFR 864.5600
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Indiana, PA, US
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